Louise Wilkins-Haug

15PUBLICATIONS

26CO-AUTHORS

Foetal development and medicineGene expression (incl. microarray and other genome-wide approaches)NeonatologyNeurogeneticsForensic epidemiology

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Publications (15)

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|Jun 11, 2026

Placental Dysfunction and Congenital Heart Disease: Investigating the Placenta-Heart Axis.

|May 19, 2026

Severe Early-Onset Fetal Growth Restriction: The Yield of Antenatal and Postnatal Genetic Testing.

|Apr 10, 2023

Postnatal genetic testing on cord blood for prenatally identified high-probability cases.

Sophie Adams, Hannah Llorin, Lori J Dobson

|Apr 06, 2023

Single gene non-invasive prenatal screening for autosomal dominant conditions in a high-risk cohort.

Sophie Adams, Hannah Llorin, Olivia Maher

|Nov 01, 2022

Prenatal diagnosis of sex chromosome aneuploidy-What do we tell the prospective parents?

Rebecca Reimers, Frances High, Jessica Kremen

|May 18, 2022

International Society for Prenatal Diagnosis Updated Position Statement on the use of genome-wide sequencing for prenatal diagnosis.

Ignatia B Van den Veyver, Natalie Chandler, Louise E Wilkins-Haug

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Frequent Collaborators

Stephanie H Guseh

Kevin G Friedman

Kathryn J Gray

Sophie J Adams

Hannah Llorin

Rebecca Reimers

Aaron R Prosnitz

Neeta L Vora

Ignatia B Van den Veyver

1 joint publications

Jacqueline G Parchem

Frequent Collaborators

Stephanie H Guseh

Kevin G Friedman

Kathryn J Gray

Sophie J Adams